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Hydrazine hydrate (1:1) → HCID 66835993, 화합물

HRID 2404450
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인쇄 미리보기

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HRID 2404450 반응식
C[O:2][C:3](=O)[CH2:4][S:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([CH:12]([C:21]2[S:22][C:23]3[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=3[N:25]=2)[O:13][CH:14]2[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]2)[CH:7]=1.O.[NH2:32][NH2:33]>C(O)C>[S:22]1[C:23]2[CH:29]=[CH:28][CH:27]=[CH:26][C:24]=2[N:25]=[C:21]1[CH:12]([O:13][CH:14]1[CH2:19][CH2:18][N:17]([CH3:20])[CH2:16][CH2:15]1)[C:8]1[CH:7]=[C:6]([S:5][CH2:4][C:3]([NH:32][NH2:33])=[O:2])[CH:11]=[CH:10][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 66835983HCID 66835983, 화합물

생성물 1

HCID 66835993HCID 66835993, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
80 °C

실험 절차

To a solution of {3-[(benzothiazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}acetic acid methyl ester (30 mg) in absolute ethanol (1 mL) is added hydrazine hydrate (0.1 mL). The reaction mixture is heated at 80° C. for 18 hours. Solvent and volatiles are removed under reduced pressure. The residue is purified by chromatography (gradient dichloromethane/methanol from 95/5 to 80/20) to give {3-[benzothiazol-2-yl(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}acetic acid hydrazide.

후처리

  1. customSolvent and volatiles are removed under reduced pressure
  2. customThe residue is purified by chromatography (gradient dichloromethane/methanol from 95/5 to 80/20)

출처 및 근거

ORD 기록
ord-52912a5d3b7b419cb52276c5b334e8c6
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802664B2

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